What are the responsibilities and job description for the Life Sciences Manufacturing Supervisor position at client.lonza.display?
Lonza is a global leader in life sciences operating across three continents. We work in science, but there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.
As a GMP Production Supervisor, you will contribute to this vision by overseeing the execution of production activities for all Cell and Gene processes at our site. This includes coordinating and supporting the execution of manufacturing procedures to comply with ET & site quality systems, as well as developing the manufacturing team to meet business needs and personal career goals.
Key Accountabilities and Duties:
- Coordinating and supporting the execution of production activities for all Cell and Gene processes at LPO to include:
- Understanding the needs of module-specific processing activities and communicating those needs to manufacturing associates on the production floor.
- Facilitating the set up and execution of manufacturing procedures to comply with ET & site quality systems.
- Developing the manufacturing team to meet business needs and personal career goals.
- Supporting the on-time in full delivery of clinical & commercial material as required.
Quality Responsibility:
Adherence to cGMPs is required at all times during the manufacture of APIs. All personnel own the quality of what they deliver and are responsible for notifying responsible management in a timely manner of regulatory inspections, serious GMP deficiencies, process deviations, product defects and related actions.
